# K232076: Fibercure

- Pathway: 510(k) (Traditional)
- Applicant: Lumendo AG
- Decided: Nov 2, 2023 after 112 days
- Product code: QNF (Laser Activator For Polymerization)
- Device class: 2
- Regulation: 21 CFR 872.6070
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K091020 (2009). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K220826: LED Curing Light, Foshan Coxo Medical Instrument Co., Ltd. (2022) Summary page 5.

## Indications for use
For light curing polymerization of small areas of dental materials capable of curing in the 385 — 425 nm wavelength range.

Source page: https://510kreport.com/device/K232076
Methodology: https://510kreport.com/methodology